Hippocampal activity in the presence of quinolones and fenbufen in vitro

Antimicrob Agents Chemother. 1991 Jun;35(6):1142-6. doi: 10.1128/AAC.35.6.1142.


Rare side effects on the central nervous system including dizziness, restlessness, and even very rare convulsions as reported during the course of antibiotic treatment with quinolones were the topic of a well-controlled in vitro approach. The excitability of brain matter was tested by electrically evoking field potentials in the CA1 region of the rat hippocampus in vitro. Direct effects of nalidixic acid, enoxacin, pefloxacin, norfloxacin, ofloxacin, and ciprofloxacin were found to occur as a dose-dependent increase in amplitude of this field potential, which is in line with the view that the quinolones increase excitability. The highest increase was found with enoxacin and nalidixic acid, and the lowest increase was found with ciprofloxacin. In order to keep the potential risk of the antibiotic therapy as low as possible, ciprofloxacin might be the drug of choice of the quinolones. In contrast to the quinolones, which only increased the amplitudes of electrically evoked potentials, fenbufen induced spontaneous firing in the pyramidal cell layer without stimulation in addition to its dose-dependent effects on the amplitudes of the evoked potentials. Threshold doses of the quinolones tested (0.25 microM) increased the amplitudes of evoked potentials in the presence of an otherwise ineffective concentration of fenbufen (1 microM) to different degrees, ranging from 39.2% for ciprofloxacin to 72.6% for enoxacin.

MeSH terms

  • 4-Quinolones
  • Animals
  • Anti-Infective Agents / pharmacology*
  • Drug Evaluation, Preclinical
  • Electric Stimulation
  • Evoked Potentials / drug effects
  • Hippocampus / drug effects*
  • In Vitro Techniques
  • Male
  • Phenylbutyrates / pharmacology*
  • Pyramidal Tracts / cytology
  • Pyramidal Tracts / drug effects
  • Rats


  • 4-Quinolones
  • Anti-Infective Agents
  • Phenylbutyrates
  • fenbufen